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Annales de genetique

Showing results (1-10 of 1,287) with videos related to

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Annales De Genetique|June 24, 2003
True hermaphroditism with 46,X,+22p/46,XY and gonadal mosaicism detected by fluorescence in situ hybridizationTakako Takano, Yasuko Yamanouchi, Fumihiko Tanaka
Annales De Genetique|January 1, 1992
Seckel syndrome: report of three sibships with the type I primordial dwarfism. Possible linkage with HLA locusG Stoppoloni, M Stabile, M M Rinaldi, et al.
Annales De Genetique|January 1, 1992
A 15p+ variant shown to be a t(Y;15) with fluorescence in situ hybridisationA A Neumann, L G Robson, A Smith
Annales De Genetique|January 1, 1992
Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotypeB Quack, N Van Roy, M R Verschraegen-Spae, et al.
Annales De Genetique|September 1, 1976
Detection of aneuploid cells in fibroblast cultures from the father of two trisomy 21 patientsG Simoni, A Mottura, M Stefanini, et al.
Annales De Genetique|January 1, 1990
An expanded mouse-human hybrid cell panel for mapping human chromosome 16D F Callen, E Baker, H J Eyre, et al.
Annales De Genetique|January 1, 1990
Cytogenetic analysis of a rare case of pediatric myxolipomaP Peulve, E Thomine, J Hemet
Annales De Genetique|January 1, 1997
Mosaic trisomy 14 with hepatic involvementA Iglesias, L D McCurdy, I A Glass, et al.
Annales De Genetique|January 1, 1996
Characterization of a de novo t(Y;9) (q11.2;q22) by FISH techniqueR A Conte, S M Kleyman, V Klein, et al.
Annales De Genetique|January 1, 1996
Myoclonic epilepsy, neuroblast migration disorders, and maternally derived partial duplication 14q/deletion 15qP Iannetti, A Spalice, R Mingarelli, et al.
Pageof 129

Showing results (1-10 of 1,287) with videos related to

Sort By:
Pageof 129
Annales De Genetique|June 24, 2003
True hermaphroditism with 46,X,+22p/46,XY and gonadal mosaicism detected by fluorescence in situ hybridizationTakako Takano, Yasuko Yamanouchi, Fumihiko Tanaka
Annales De Genetique|January 1, 1992
Seckel syndrome: report of three sibships with the type I primordial dwarfism. Possible linkage with HLA locusG Stoppoloni, M Stabile, M M Rinaldi, et al.
Annales De Genetique|January 1, 1992
A 15p+ variant shown to be a t(Y;15) with fluorescence in situ hybridisationA A Neumann, L G Robson, A Smith
Annales De Genetique|January 1, 1992
Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotypeB Quack, N Van Roy, M R Verschraegen-Spae, et al.
Annales De Genetique|September 1, 1976
Detection of aneuploid cells in fibroblast cultures from the father of two trisomy 21 patientsG Simoni, A Mottura, M Stefanini, et al.
Annales De Genetique|January 1, 1990
An expanded mouse-human hybrid cell panel for mapping human chromosome 16D F Callen, E Baker, H J Eyre, et al.
Annales De Genetique|January 1, 1990
Cytogenetic analysis of a rare case of pediatric myxolipomaP Peulve, E Thomine, J Hemet
Annales De Genetique|January 1, 1997
Mosaic trisomy 14 with hepatic involvementA Iglesias, L D McCurdy, I A Glass, et al.
Annales De Genetique|January 1, 1996
Characterization of a de novo t(Y;9) (q11.2;q22) by FISH techniqueR A Conte, S M Kleyman, V Klein, et al.
Annales De Genetique|January 1, 1996
Myoclonic epilepsy, neuroblast migration disorders, and maternally derived partial duplication 14q/deletion 15qP Iannetti, A Spalice, R Mingarelli, et al.
Pageof 129